Nanoparticle-aptamer bioconjugates for cancer targeting

被引:208
作者
Farokhzad, Omid C. [1 ,2 ]
Karp, Jeffrey M. [3 ]
Langer, Robert [4 ]
机构
[1] Brigham & Womens Hosp, Dept Anesthesiol Perioperat & Pain Med, Boston, MA 02115 USA
[2] Harvard Univ, Sch Med, Boston, MA 02115 USA
[3] MIT, Dept Chem Engn, Cambridge, MA 02139 USA
[4] MIT, Dept Chem Engn, Cambridge, MA 02139 USA
关键词
aptamer; cancer therapy; controlled release; in vitro selection; nanoparticles; SELEX; targeted drug delivery;
D O I
10.1517/17425247.3.3.311
中图分类号
R9 [药学];
学科分类号
1007 ;
摘要
The combination of targeted drug delivery and controlled-release technology may pave the road for more effective yet safer chemotherapeutic options for cancer therapy. Drug-encapsulated polymeric nanoparticle-aptamer bioconjugates represent an emerging technology that can facilitate the delivery of chemotherapeutics to primary and metastatic tumours. Aptamers are short nucleic acid molecules with binding properties and biochemical characteristics that may make them suitable for use as targeting molecules. The goal of this review is to summarise the key components that are required for creating effective cancer targeting nanoparticle-aptamer bioconjugates. The field of controlled release and the structure and properties of aptamers, as well as the criteria for constructing effective conjugates, will be discussed.
引用
收藏
页码:311 / 324
页数:14
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